DNA, Complementary < DNA, Mitochondrial < DNA, Recombinant

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List of bibliographic references

Number of relevant bibliographic references: 22.
[0-20] [0 - 20][0 - 22][20-21][20-40]

Ident.	Authors (with country if any)	Title
000054 (1999)	L. Sudarsky [États-Unis] ; G M Plotkin ; E L Logigian ; D R Johns	Dystonia as a presenting feature of the 3243 mitochondrial DNA mutation.
000134 (1999)	P. Chariot [France] ; P. Brugières ; M C Eliezer-Vanerot ; C. Gény ; M. Binaghi ; P. Césaro	Choreic movements and MRI abnormalities in the subthalamic nuclei reversible after administration of coenzyme Q10 and multiple vitamins in a patient with bilateral optic neuropathy.
000A89 (2003)	Ying Peng [États-Unis] ; Roger Crumley ; John M. Ringman	Spasmodic dysphonia in a patient with the A to G transition at nucleotide 8344 in mitochondrial DNA.
000D43 (2004)	Michael D. Brown [États-Unis] ; Seyed Hosseini ; Israel Steiner ; Douglas C. Wallace ; Isabelle Korn-Lubetzki	Complete mitochondrial DNA sequence analysis in a family with early-onset dystonia and optic atrophy.
001295 (2005)	Maher A. Noureddine [États-Unis] ; Yi-Ju Li ; Joelle M. Van Der Walt ; Robert Walters ; Rita M. Jewett ; Hong Xu ; Tianyuan Wang ; Jeffrey W. Walter ; Burton L. Scott ; Christine Hulette ; Don Schmechel ; Judith E. Stenger ; Fred Dietrich ; Jeffery M. Vance ; Michael A. Hauser	Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra.
001B28 (2007)	Robert A. Wilcox [Australie] ; Andrew Churchyard ; Henrik H. Dahl ; Wendy M. Hutchison ; Denise M. Kirby ; Dominic Thyagarajan	Levodopa response in Parkinsonism with multiple mitochondrial DNA deletions.
001E66 (2008)	Maria Stella Aniello [Italie] ; Davide Martino ; Vittoria Petruzzella ; Roberto Eleopra ; Michelangelo Mancuso ; Rosa Dell'Aglio ; Michele Cavallo ; Gabriele Siciliano ; Giovanni Defazio	Bilateral striatal necrosis, dystonia and multiple mitochondrial DNA deletions: case study and effect of deep brain stimulation.
002105 (2008)	Hélio A G. Teive ; Renato P. Munhoz ; Juliano A. Muzzio ; Rosana H. Scola ; Cláudia K. Kay ; Salmo Raskin ; Lineu C. Werneck ; Helene Bruhn	Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case report.
002251 (2008)	Michelangelo Mancuso ; Daniele Orsucci ; Sara Gori ; Roberto Ceravolo ; Gabriele Siciliano	Mitochondrial DNA single deletion in a patient with postural tremor.
002453 (2009)	Prachi Mehta [Australie] ; George D. Mellick ; Dominic B. Rowe ; Glenda M. Halliday ; Michael M. Jones ; Neil Manwaring ; Himesha Vandebona ; Peter A. Silburn ; Jie Jin Wang ; Paul Mitchell ; Carolyn M. Sue	Mitochondrial DNA haplogroups J and K are not protective for Parkinson's disease in the Australian community.
002840 (1990)	A H Schapira [Royaume-Uni] ; I J Holt ; M. Sweeney ; A E Harding ; P. Jenner ; C D Marsden	Mitochondrial DNA analysis in Parkinson's disease.
002968 (2010)	Lisa S. Friedman [États-Unis] ; Jennifer M. Farmer [États-Unis] ; Susan Perlman [États-Unis] ; George Wilmot [États-Unis] ; Christopher Gomez [États-Unis] ; Khalaf O. Bushara [États-Unis] ; Katherine D. Mathews [États-Unis] ; S. H. Subramony [États-Unis] ; Tetsuo Ashizawa [États-Unis] ; Laura J. Balcer [États-Unis] ; Robert B. Wilson [États-Unis] ; David R. Lynch [États-Unis]	Measuring the rate of progression in Friedreich ataxia: Implications for clinical trial design
002F43 (2011)	Arpan R. Mehta [Canada] ; Susan H. Fox ; Mark Tarnopolsky ; Grace Yoon	Mitochondrial mimicry of multiple system atrophy of the cerebellar subtype.
003020 (2011)	Josef Finsterer [Autriche]	Parkinson's syndrome and Parkinson's disease in mitochondrial disorders.
003D42 (2013)	Claude Vital [France] ; Anne Vital	Are substantia nigra neurons subject to mitochondrial dysfunction in early life more able to adapt?
004767 (1994)	H. Reichmann [Allemagne] ; M. Naumann ; S. Hauck ; B. Janetzky	Respiratory chain and mitochondrial deoxyribonucleic acid in blood cells from patients with focal and generalized dystonia.
004774 (1994)	G. Lera [Royaume-Uni] ; K. Bhatia ; C D Marsden	Dystonia as the major manifestation of Leigh's syndrome.
004889 (1994)	A H Schapira ; C D Marsden	Platelet mitochondrial DNA in Parkinson's disease.
004904 (1994)	A H Schapira [Royaume-Uni]	Evidence for mitochondrial dysfunction in Parkinson's disease--a critical appraisal.
004A03 (1993)	M S Sandy ; J W Langston ; M T Smith ; D A Di Monte	PCR analysis of platelet mtDNA: lack of specific changes in Parkinson's disease.
004D70 (1997)	S. Kösel [Allemagne] ; R. Egensperger ; N M Schnopp ; M B Graeber	The 'common deletion' is not increased in parkinsonian substantia nigra as shown by competitive polymerase chain reaction.

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